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Indero
Overview
The Senior CRA monitors clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP guidelines. Responsibilities include conducting site visits, performing source data verification, and potentially mentoring other CRAs as a Lead CRA.
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Compensation
Salary not listed
Posted
9 days ago
IQVIA
Coordinate clinical research studies by performing complex clinical procedures and managing subject well-being. Responsibilities include recruiting volunteers, administering study drugs, and ensuring data accuracy in accordance with protocols.
CA$40 - CA$50 / HOUR
26 days ago
Centricity Research
The Clinical Research Coordinator will support study execution by performing clinical procedures, managing participant safety, and ensuring compliance with protocols and regulatory requirements. They will also handle recruitment, screening, and data documentation to maintain high standards of study integrity.
1 month ago
Syneos Health
The Research Nurse will be fully conversant with the trial protocol, ensuring accurate documentation, data transfer, and adherence to GCP throughout the study. Key duties include coordinating subject visits, administering trial medication, assisting with patient recruitment, and accurately reporting adverse events.
2 months ago
